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Water → 2-(4-Bromophenyl)-3,3,3-trifluoronitropropene

HRID 1057985
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HRID 1057985 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[C:9]([F:12])([F:11])[F:10])=[CH:4][CH:3]=1.[CH3:14][N+:15]([O-:17])=[O:16].O>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:9]([F:12])([F:11])[F:10])=[CH:14][N+:15]([O-:17])=[O:16])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6375NitromethaneHCID 6038664'-Bromo-2,2,2-trifluoroacetophenone

생성물 1

HCID 536841792-(4-Bromophenyl)-3,3,3-trifluoronitropropene

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A stirred solution of 4′-bromo-2,2,2-trifluoroacetophenone (0.392 g, 2.00 mmol). and CH3NO2 (0.488 g, 8.0 mmol) in dry toluene (70 mL) containing N,N-diethylenediamine (30 mmol) is heated at reflux with a Dean and Stark trap until complete removal of H2O. The cooled solution is washed with 5% aqueous HCl, dried over MgSO4, filtered, evaporated in vacuo and the resulting residue when purified by chromatography gives the title compound.

후처리

  1. temperatureis heated
  2. washThe cooled solution is washed with 5% aqueous HCl
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. customevaporated in vacuo
  6. customthe resulting residue when purified by chromatography

출처 및 근거

ORD 기록
ord-6bf34d7644d3454d8bc9f17ebaa6e019
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06515026B2

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